Structural, spectroscopic, and biological aspects of S∩N donor Schiff-base ligands and their chromium(III) complexes

Abstract

New chromium(III) complexes are synthesized by classical thermal and microwave (MW)-irradiated techniques. The Schiff bases 2-acetylfuran-S-benzyldithiocarbazate (L1H), 2-acetylthiophene-S-benzyldithiocarbazate (L2H), 2-acetylpyridine-S-benzyldithiocarbazate (L3H), and 2-acetylnaphthalene-S-benzyldithiocarbazate (L4H) were prepared by condensation of -S-benzyldithiocarbazate in ethanol with the respective ketones by using MW as well as conventional methods. The chromium(III) complexes have been prepared by mixing CrCl3 · 6H2O in 1 : 1 and 1 : 2 molar ratios with monofunctional bidentate ketimines. The structure of the ligands and their transition metal complexes were confirmed by elemental analysis, melting point determinations, molecular weight determinations, infrared (IR), electronic and electron paramagnetic resonance (EPR) spectral, and X-ray powder diffraction studies. On the basis of these studies it is clear that the ligands coordinated to the metal atom in a monobasic bidentate mode by S∩N donors. Thus, an octahedral environment around the chromium(III) has been proposed. The growth inhibiting potential of the ligands and complexes has been assessed against a variety of fungal and bacterial strains.